US20220002628A1 - Emulsifer and emulsions - Google Patents
Emulsifer and emulsions Download PDFInfo
- Publication number
- US20220002628A1 US20220002628A1 US17/436,470 US202017436470A US2022002628A1 US 20220002628 A1 US20220002628 A1 US 20220002628A1 US 202017436470 A US202017436470 A US 202017436470A US 2022002628 A1 US2022002628 A1 US 2022002628A1
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- US
- United States
- Prior art keywords
- diesel
- fatty acid
- composition
- emulsifier
- water
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000839 emulsion Substances 0.000 title abstract description 69
- 239000003995 emulsifying agent Substances 0.000 claims abstract description 72
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 61
- 239000000446 fuel Substances 0.000 claims abstract description 40
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 37
- 239000000194 fatty acid Substances 0.000 claims abstract description 37
- 229930195729 fatty acid Natural products 0.000 claims abstract description 37
- -1 C24 fatty acid Chemical class 0.000 claims abstract description 26
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 26
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 11
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000000203 mixture Substances 0.000 claims description 72
- 239000002516 radical scavenger Substances 0.000 claims description 30
- 239000010763 heavy fuel oil Substances 0.000 claims description 25
- 239000007908 nanoemulsion Substances 0.000 claims description 22
- 239000005864 Sulphur Substances 0.000 claims description 21
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 18
- 239000002283 diesel fuel Substances 0.000 claims description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 17
- 239000003225 biodiesel Substances 0.000 claims description 10
- 238000004945 emulsification Methods 0.000 claims description 7
- 230000001804 emulsifying effect Effects 0.000 claims description 6
- 235000021281 monounsaturated fatty acids Nutrition 0.000 claims description 6
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 238000009472 formulation Methods 0.000 claims description 4
- 238000000034 method Methods 0.000 abstract description 6
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 abstract description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 239000007789 gas Substances 0.000 description 8
- 239000005022 packaging material Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 6
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 5
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 5
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- 239000005642 Oleic acid Substances 0.000 description 5
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 5
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 235000019198 oils Nutrition 0.000 description 5
- 235000021313 oleic acid Nutrition 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- 230000009286 beneficial effect Effects 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 150000001735 carboxylic acids Chemical class 0.000 description 4
- 235000019864 coconut oil Nutrition 0.000 description 4
- 239000003240 coconut oil Substances 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229920000847 nonoxynol Polymers 0.000 description 4
- 239000013618 particulate matter Substances 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 3
- QFMDFTQOJHFVNR-UHFFFAOYSA-N 1-[2,2-dichloro-1-(4-ethylphenyl)ethyl]-4-ethylbenzene Chemical compound C1=CC(CC)=CC=C1C(C(Cl)Cl)C1=CC=C(CC)C=C1 QFMDFTQOJHFVNR-UHFFFAOYSA-N 0.000 description 3
- IEORSVTYLWZQJQ-UHFFFAOYSA-N 2-(2-nonylphenoxy)ethanol Chemical compound CCCCCCCCCC1=CC=CC=C1OCCO IEORSVTYLWZQJQ-UHFFFAOYSA-N 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- NWGKJDSIEKMTRX-AAZCQSIUSA-N Sorbitan monooleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-AAZCQSIUSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- ZBJVLWIYKOAYQH-UHFFFAOYSA-N naphthalen-2-yl 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=C(C=CC=C2)C2=C1 ZBJVLWIYKOAYQH-UHFFFAOYSA-N 0.000 description 3
- 239000001593 sorbitan monooleate Substances 0.000 description 3
- 235000011069 sorbitan monooleate Nutrition 0.000 description 3
- 229940035049 sorbitan monooleate Drugs 0.000 description 3
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- 235000019482 Palm oil Nutrition 0.000 description 2
- 229910000420 cerium oxide Inorganic materials 0.000 description 2
- 239000010779 crude oil Substances 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000003344 environmental pollutant Substances 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 2
- 239000002540 palm oil Substances 0.000 description 2
- 231100000719 pollutant Toxicity 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 2
- CUNWUEBNSZSNRX-RKGWDQTMSA-N (2r,3r,4r,5s)-hexane-1,2,3,4,5,6-hexol;(z)-octadec-9-enoic acid Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O CUNWUEBNSZSNRX-RKGWDQTMSA-N 0.000 description 1
- POAOYUHQDCAZBD-IDEBNGHGSA-N 2-butoxyethanol Chemical group [13CH3][13CH2][13CH2][13CH2]O[13CH2][13CH2]O POAOYUHQDCAZBD-IDEBNGHGSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 239000004147 Sorbitan trioleate Substances 0.000 description 1
- PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- FGUZFFWTBWJBIL-XWVZOOPGSA-N [(1r)-1-[(2s,3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)O[C@H](CO)[C@H]1OC[C@H](O)[C@H]1O FGUZFFWTBWJBIL-XWVZOOPGSA-N 0.000 description 1
- IJCWFDPJFXGQBN-RYNSOKOISA-N [(2R)-2-[(2R,3R,4S)-4-hydroxy-3-octadecanoyloxyoxolan-2-yl]-2-octadecanoyloxyethyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCCCCCCCCCCCC IJCWFDPJFXGQBN-RYNSOKOISA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 235000019387 fatty acid methyl ester Nutrition 0.000 description 1
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N linoleic acid group Chemical group C(CCCCCCC\C=C/C\C=C/CCCCC)(=O)O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000004530 micro-emulsion Substances 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 229940057429 sorbitan isostearate Drugs 0.000 description 1
- 229960005078 sorbitan sesquioleate Drugs 0.000 description 1
- 235000019337 sorbitan trioleate Nutrition 0.000 description 1
- 229960000391 sorbitan trioleate Drugs 0.000 description 1
- 239000001589 sorbitan tristearate Substances 0.000 description 1
- 235000011078 sorbitan tristearate Nutrition 0.000 description 1
- 229960004129 sorbitan tristearate Drugs 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
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- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/017—Mixtures of compounds
- C09K23/018—Mixtures of two or more different organic oxygen-containing compounds
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- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/34—Higher-molecular-weight carboxylic acid esters
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- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
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- C10L1/188—Carboxylic acids; metal salts thereof
- C10L1/189—Carboxylic acids; metal salts thereof having at least one carboxyl group bound to an aromatic carbon atom
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- C10L1/1985—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyethers, e.g. di- polygylcols and derivatives; ethers - esters
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- C10L1/00—Liquid carbonaceous fuels
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- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
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- C10L2200/0407—Specifically defined hydrocarbon fractions as obtained from, e.g. a distillation column
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- C10L2200/0461—Fractions defined by their origin
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- C10L2250/00—Structural features of fuel components or fuel compositions, either in solid, liquid or gaseous state
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- C10L2250/00—Structural features of fuel components or fuel compositions, either in solid, liquid or gaseous state
- C10L2250/08—Emulsion details
- C10L2250/086—Microemulsion or nanoemulsion
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- C10L2270/00—Specifically adapted fuels
- C10L2270/02—Specifically adapted fuels for internal combustion engines
- C10L2270/026—Specifically adapted fuels for internal combustion engines for diesel engines, e.g. automobiles, stationary, marine
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- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L2290/00—Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
- C10L2290/24—Mixing, stirring of fuel components
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- C10L2290/00—Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
- C10L2290/34—Applying ultrasonic energy
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/10—Biofuels, e.g. bio-diesel
Definitions
- This invention relates to compositions suitable for use as emulsifiers or scavengers and to diesel formulations or emulsions containing the compositions.
- Diesel engines are very efficient engines. However, the use of diesel fuel presents a number of difficulties. In particular, diesel engines produce a significant amount of regulated pollutants, including particulate matter, NOx, SOx and CO.
- water-emulsified diesel can improve the physical or chemical properties of the diesel and reduce some of the pollutant emissions.
- Lif and Holmberg “Water-in-diesel emulsions and related systems”, Advances in Colloid and Interface Science, 123-126 (2006), pp 231-239 provides background of the use of water-emulsified diesel and other related fuels.
- WO2013/098630 discloses diesel oil and water emulsions and discusses the importance of stability of at least 3 months under normal storage conditions and at temperatures between ⁇ 20 and +50° C. However, there is no evidence of an improved stability.
- WO03/075954 discloses and emulsifying composition comprising an ethoxylated alkylphenol, a fatty acid amine, oleic acid and naphtha.
- Diesel fuels typically contains large amounts of sulphur, which results in the production of SOx. There is a move to reduce the amount of sulphur present in diesel. However, reducing the amount of sulphur also reduces the lubricity of the diesel, which causes problems in the engine, as discussed in Uchoa et al, “Evaluation of Lubricating Properties of Diesel Based Fuels Micro Emulsified With Glycerin”, Materials Research, 2017, 20(Suppl. 2), pp 701-708. This is commonly remedied by including bio-ingredients into the diesel fuel. However, the inclusion of these bio-ingredients can cause problems with the formation of stable nano-emulsions.
- compositions which are capable of forming stable nano-emulsions in standard diesel are not typically capable of forming stable nano-emulsions in ultra low sulphur diesel with bio-ingredients and vice versa.
- composition which can be tailored easily to produce stable nano-emulsions in diesel fuels containing different amounts of sulphur and different amounts of bio-components.
- compositions which can be tailored to improve different properties of the emulsions, including lubricity, droplet size, corrosion resistance and specific gaseous and particulate emissions.
- composition which is capable of producing a stable nano-emulsion at low levels of power input and/or very quickly.
- diesel or diesel fuel is intended to cover petroleum diesel, low-sulphur diesel, biodiesel and combinations thereof.
- reference to petroleum diesel relates to diesel produced during the distillation of crude oil.
- reference to heavy fuel oil relates to oil produced during the distillation of crude oil and having a density greater than 900 kg/m 3 at 15° C.
- low-sulphur diesel relates to diesel having less than 500 ppm, preferably less than 50 ppm, and most preferably less than 10 ppm sulphur.
- Low-sulphur diesel can be produced by removing the sulphur from petroleum diesel, by the formation of synthetic diesel or by the formation of biodiesel.
- biodiesel relates to fatty acid methyl ester obtained by transesterification of vegetable oils or animal fats with an alcohol, typically methanol or ethanol.
- bio-components relates to biodiesel and naturally occurring oils, such as palm oil, rapeseed oil and coconut oil.
- an emulsifier which is capable of forming a stable emulsion with diesel or heavy fuel oil.
- the emulsifier comprises:
- the emulsifier does not comprise or contain naphtha.
- the emulsifier consists essentially of components (a), (b) and (c).
- the emulsifier is suitable to be used to form an emulsion with diesel, low sulphur diesel, biodiesel or heavy fuel oil.
- the emulsion can comprise up to 30 wt % water.
- the emulsion comprises at least 0.5 wt % emulsifier. Higher levels of emulsifier can be used up to 15 wt %. However, increasing the amount of emulsifier increases the cost with no identifiable improvement in stability. Therefore, a preferred upper limit for the amount of emulsifier is 3 wt %. It is preferred that the emulsion contains only the fuel, water and the emulsifier.
- the fatty acid diethanolamide is a formed from a mixture of fatty acids having from 8 to 18 carbon atoms. It is particularly preferred that the fatty acid diethanolamide is derived from a natural source. Suitable natural sources include coconut oil and palm oil. By way of example, coconut oil is a mixture of acids including caprylic, capric, lauric, myristic, palmitic, stearic, oleic and linoleic acids.
- HLB One feature of components used in emulsifiers is the HLB.
- HLB values can either be calculated or determined experimentally. The standard methods of calculation include those of Griffin (Journal of the Society of Cosmetic Chemists 5 (1654): 259) or Davies (Gas/Liquid and Liquid/Liquid interface: Proceedings of the International Congress of the Surface Activity (1657). However, it is preferred that the HLB values are obtained experimentally. It is usual for suppliers of materials to provide HLB values for their products which are obtained experimentally. The skilled person is aware of suitable methods to determine the HLB value, such as using comparative testing by forming a series of emulsions with an emulsifier and an oil of known HLB value. In general, a HLB in the range of 3.5 to 6 is commonly used for water in oil emulsions. A HLB in the range of 8 to 18 is used for oil in water emulsions.
- coconut oil diethanolamide typically has a HLB in the range of 13-14. Whilst it is not essential that the diethanolamide has an HLB in this range, it is preferred that the diethanolamide has an HLB in the range of 11-16 and preferably 13-14.
- Fatty acid diethanolamides based on fatty acids with fewer than 8 carbon atoms or more than 18 carbon atoms can optionally be present in the mixture, although it is preferred that they are not.
- the fatty acid diethanolamide is present in an amount of from 40 to 90 wt % of the emulsifier. It is more preferred that it is present in an amount of from 50 to 90 wt % and more preferably from 60 to 85 wt %.
- the at least one C 12 to C 24 fatty acid is preferably saturated or monounsaturated, with monounsaturated fatty acids being further preferred.
- the fatty acid is preferably a C 14-20 monounsaturated fatty acid.
- a particularly suitable fatty acid is oleic acid.
- Oleic acid has a HLB of approximately 1.
- a low HLB means that it is highly lipophilic and therefore a material of this lipophilicity is not typically used as an emulsifier. It is preferred that the fatty acid has a low HLB, preferably below 3.5 and more preferably below 2.
- the fatty acids are preferably present in an amount of from 1 to 15 wt %, more preferably from 2 to 10 wt % and most preferably from 4 to 7 wt % of the emulsifier.
- the C 6 to C 18 alcohol ethoxylate is preferably produced from at least one alcohol and more preferably at least one mono-ol.
- the ethoxylates preferably have from 2 to 8 ethoxy-groups.
- Preferred ethoxylates include nonylphenol ethoxylate and C 9 -C 12 ethoxylates.
- Suitable ethoxylates are commercially available.
- Suitable ethoxylates include Berol 260 and Ethylan 1005, which are narrow range ethoxylated alcohols commercially available from AkzoNobel.
- Nonylphenol ethoxylates have a range of HLB values depending on the number of ethylene oxide groups present.
- Preferred nonylphenol ethoxylate have from 4 to 8 ethylene oxide groups, which have an HLB of approximately from 9 to 12.
- a particularly preferred nonylphenol ethoxylate has 6 ethylene oxide groups and a HLB of approximately 11.
- Berol 260 has a HLB value of 10.5 and is a narrow range C 9 -11 alcohol with 4 ethylene oxide groups.
- Ethylan 1005 has a HLB value of 11.6 and is a narrow range C 10 alcohol with 3.5 ethylene oxide groups.
- the alcohol ethoxylate has a HLB value in the range of 9 to 12 and preferably from 10 to 12.
- the alcohol ethoxylate is preferably present in an amount of from 5 to 30 wt % of the emulsifier. It is further preferred that the alcohol ethoxylate is present in an amount of from 5 to 20 wt % and more preferably from 8 to 12 wt %.
- the emulsifier can optionally comprise a sorbitan ester as defined below.
- the sorbitan ester where present, is used in an amount of from 10 to 40 wt % of the emulsifier, preferably from 20 to 30 wt %.
- an emulsifier which is suitable for forming a stable nano-emulsion of diesel and water, wherein the diesel does not contain any bio-components.
- the emulsifier comprises:
- Preferred components a to c are as defined above.
- the emulsifier does not comprise naphtha.
- the emulsifier consists essentially of components (a), (b) and (c).
- the nano-emulsion comprises a fuel comprising at least one of petroleum diesel, low sulphur diesel and heavy fuel oil, wherein the fuel does not contain any bio-components, wherein the fuel does not contain any bio-components, up to 20 wt % water and the emulsifier, wherein the emulsifier:water volume ratio is from 1.5:1 to 1:2.9, and preferably 1.2:1 to 1:2. It is preferred that the water is present in an amount of at least 0.25 wt % and more preferably at least 0.5 wt %. It is preferred that the nano-emulsion contains only the fuel, water and emulsifier. Although other components can be present, it is preferred that these are only present in trace amounts of less than 0.1 wt %.
- the emulsifier of the second aspect comprises 80-90 wt % of component a, 4-8 wt % of component b and 5-15 wt % of component c.
- an emulsifier which is suitable for forming a stable nano-emulsion of diesel and water, wherein the diesel contains bio-components.
- the emulsifier comprises:
- the emulsifier does not comprise or contain naphtha.
- the emulsifier consists essentially of components (a), (b), (c) and (d).
- the nano-emulsion comprises a fuel comprising at least one of diesel, low sulphur diesel, biodiesel and heavy fuel oil, wherein the fuel comprises bio-components, up to 20 wt % water and the emulsifier of the third aspect.
- the emulsifier:water volume ratio is from 1.5:1 to 1:2.9, and preferably 1.2:1 to 1:2. It is preferred that the nano-emulsion contains only the fuel, water and emulsifier. Although other components can be present, it is preferred that these are only present in trace amounts of less than 0.1 wt %.
- Preferred components a to c are as defined above.
- the sorbitan ester is the reaction product of sorbitan and one or more carboxylic acids.
- the carboxylic acids have from 8 to 22 carbon atoms.
- the carboxylic acids have from 8 to 22 carbon atoms, which is the length of carbon chains found in naturally occurring fatty acids in triglycerides.
- Particularly preferred are carboxylic acids having from 16 to 22 carbon atoms and even more preferably having 18 carbon atoms.
- the fatty acids can be both linear and branched.
- Both saturated and unsaturated fatty acids are suitable. However, unsaturated fatty acids are preferred.
- sorbitan esters which are suitable for use in the present invention include:
- Suitable sorbitan esters have an HLB of less than 6.0.
- Preferred sorbitan esters are those having an HLB of from 3 to 5. Particularly preferred is sorbitan monooleate.
- the emulsifier of the second aspect comprises 55-65 wt % of component a, 4-8 wt % of component b, 5-15 wt % of component c and 20 to 30 wt % of component d.
- a scavenger solution is capable of being added to diesel or heavy fuel oil.
- the scavenger solution is capable of emulsifying any residual water in the diesel as well as improving the lubricity of the diesel. By removal of residual water, the scavenger is capable of providing other benefits including preventing diesel bug.
- the scavenger solution comprises:
- the scavenger solution does not comprise or contain naphtha
- the scavenger solution consists essentially of components (a), (b), (c) and (d).
- the scavenger solution comprises from 10 to 40 wt % of the emulsifier of any one of the first to third aspects of the present invention and from 60 to 90 wt % alkylene glycol monoalkyl ether.
- a fuel formulation is formed of a fuel comprising at least one of diesel, low sulphur diesel, biodiesel and heavy fuel oil and the scavenger solution in an amount of 0.03 to 0.2% by volume and preferably 0.03 to 0.075% by volume.
- the inclusion of the scavenger in the above amounts is capable of treating a fuel with up to 5 wt % of residual water. However, it is preferred that the water contains less than 2.5 wt % and more preferably less than 1 wt % water.
- the fuel formulation contains only the fuel, water and emulsifier. Although other components can be present, it is preferred that these are only present in trace amounts of less than 0.1 wt %.
- Preferred components a to c are as defined above.
- the alkylene glycol monoalkyl ether is preferably an ethylene glycol monoalkyl ether and more preferably an ethylene glycol monoalkyl ether in which the alkyl group has from 1 to 6 carbon atoms. More preferably, the ether is preferably 2-butoxyethanol (butyl oxitol).
- the alkylene glycol monoalkyl ether is preferably used in an amount of 70 to 90% by weight and more preferably from 75 to 85% by weight.
- the emulsifiers of the present invention advantageously permit emulsions of diesel and heavy fuel oils to be formed easily with low levels of emulsification energy.
- the resulting emulsions produced are stable for long periods of time.
- the emulsions also provide the advantageous properties of water in diesel emulsions by reducing the amount of emissions and particulates produced.
- These emulsifiers which can be produced using naturally occurring materials, are therefore beneficial as they are environmentally beneficial as they do not typically contain components which are harmful to produce whilst at the same time reducing emissions in the engines in which they are used.
- Emulsions can be formed irrespective of the order of the addition. It is possible to add the emulsifier to the diesel or heavy fuel oil and then add water, to add the emulsifier to a mixture of diesel or heavy fuel oil and water or to add a mixture of emulsifier and water to the diesel or heavy fuel oil.
- a mixture of an emulsifier according to any one of the above aspects of the present invention and water comprises water and emulsifier in the relative amounts described above in the absence of the diesel or heavy fuel oil.
- a method of making a nano-emulsion comprising emulsifying a mixture of fuel, water and an emulsifier of the second, third or fourth embodiments using ultrasonic emulsification.
- One benefit of forming a nano-emulsion using ultrasonic emulsification is the speed at which the emulsions can be produced.
- the emulsions can be formed in seconds rather than minutes.
- nano-emulsions of water in diesel have been shown to be effective for use in diesel engines at reducing the level of toxic emissions.
- the emulsions of the present invention are not only highly stable, but the nano-emulsions can be produced using surprisingly low levels of energy, which is commercially and environmentally advantageous.
- the scavenger solution of the fourth aspect can be used to produce nano-emulsions, it is preferred that the emulsion is produced by simple addition of the scavenger solution to the fuel.
- the emulsions can be formed by simple mixing of the scavenger solution and fuel.
- the emulsion can form in situ as the fuel passes through the fuel pump.
- the emulsifier or scavenger compositions of any of the first to fourth aspects can optionally contain other components.
- the inclusion of the components is generally known to the skilled person and they are used in their usual amounts.
- Metal oxides are known to be useful for reducing SOx and NOx. Where used, these are typically present in the compositions in amounts of from 5 to 100 ppm. Suitable metal oxides include cerium oxide, magnesium oxide, titanium oxide, iron oxide and aluminium oxide. Magnesium oxide is typically used in heavy fuel oils and cerium oxide is typically used in diesel.
- Ferrocene is also known to the skilled person to be useful for promoting smokeless combustion of fuels.
- Lower (C 1-5 ) alcohols are commonly used to reduce soot and also to reduce the freezing point of the diesel or heavy fuel oil composition.
- Preferred alcohols include methanol, ethanol, i-propanol and n-propanol. These are used in an amount of less than 5% by weight and more preferably less than 2% by weight.
- Stability of the emulsions is important. A simple emulsion of water and diesel will slowly separate. The inclusion of emulsifiers is therefore intended to improve the stability.
- One measure of the stability of the emulsion is the droplet size. This can be measured by looking at the turbidity, which can be measured using a Turbimeter, such as a Van Walt Compact Turbimeter. Therefore, turbidity can be used as a means of studying the stability of an emulsion.
- the turbidity can be used to assess how effective an emulsifier is at forming an emulsion i.e. the relative ability of an amount of emulsifier to form an emulsion. The smaller the particle size for a specific amount of emulsifier, the more effective that emulsifier is.
- Measurement of turbidity is a quick method to establish the effectiveness of an emulsifier.
- FIG. 1 shows the stability of diesel emulsions over a year
- FIG. 2 shows the stability of a diesel emulsion when cooled to ⁇ 20° C.
- FIG. 3 shows the stability of a diesel emulsion when heated to 70° C.
- FIG. 4 shows the stability of a heavy fuel oil emulsion after 9 months.
- compositions were produced and tested for producing emulsions with varying amounts of water. Each composition was produced by mixing the emulsifier, blending the emulsifier with diesel and then adding water and emulsifying.
- the emulsifiers were made using the following ingredients:
- Sorbitan monooleate (SPAN 80) by CRODA®
- the emulsifiers used the following parts by weight.
- SC is a Heidolph Silent Crusher variable speed high shear mixer.
- U1000 is a Hielscher UIP1000 bench top ultrasonicator.
- U400 is a Hielscher UP400st lab ultrasonicator.
- Shell 50 is Shell V Power 50 ppm diesel which has less than 50 ppm sulphur and contains bio-components.
- Turbidity was measured immediately after the formation of the emulsion using the Van Walt Compact Turbimeter.
- compositions of the present invention are capable of forming stable emulsions with low turbidity across a broad range of water content using low levels of the compositions.
- the compositions are also capable of forming stable emulsions even when the fuel is a low sulphur fuel.
- compositions were tested to measure the stability of emulsions of water and diesel containing biocomponents at higher levels of water.
- Composition 10 was mixed with water at a ratio of 33 parts composition to 67 parts by weight water. The mixture of water and composition were then added to Shell 50 in the amounts set out in Table 3. The mixing was undertaken at ambient temperature. The diesel/water mixture was emulsified using a U400 ultrasonicator for 1 minute. The samples were then allowed to cook to ambient temperature and transferred to a container for long term storage. The container was stored at ambient temperature at an altitude of 550 m. The ambient temperature varied from 0° C. to 37° C.
- the turbidity was measured immediately after emulsification and again after a few minutes once air bubbles had cleared.
- the emulsions were stored for a period of greater than a year. It should be noted that storage of modern fuels for more than 6 months is not recommended. All three emulsions were stable for a year. After 15 months, the emulsion containing 10 pbw water/emulsifier had separated slightly. This was the time when the first signs of separation had started to show. 15 months is an extremely long period of stability. This is shown in FIG. 1 , in which a) shows the emulsions at formation (water/emulsifier content from left to right 20, 15, 10) and b) shows the emulsions after 15 months (same order) in which the emulsion for 10 pbw water is more turbid.
- Example 10 5 parts by weight of Example 10 was mixed with 85 parts by weight of diesel and 10 parts by weight of water.
- the diesel/water/emulsifier mixture was emulsified using a U400 ultrasonicator for 1 minute.
- the samples were placed in a heated oven at 70° C. for 1 hour and returned to ambient temperature.
- the same samples were placed in a freezer at ⁇ 20° C. for an hour and returned to ambient temperature.
- the emulsion is turbid.
- the emulsion is clear after returning to ambient temperature without stirring.
- Example 7 1 part by weight of the composition of Example 7 was mixed with 30 parts by weight of water and 69 parts by weight of heavy fuel oil at 70° C. and emulsified using a U400 ultrasonicator for 3.5 minutes. The samples were then allowed to cool to ambient temperature and transferred to a container for long term storage. The container was stored at ambient temperature at an altitude of 550 m. The ambient temperature varied from 0° C. to 37° C.
- FIG. 4 shows the emulsion of the heavy fuel oil and water after 9 months.
- a scavenger solution was prepared using Composition 7. 1 part by weight of this composition was mixed with 4 parts by weight of butyl oxitol.
- the diesel generator was a 229-3 3 cylinder generator from MWM Motores Diesel Ltda.
- the scavenger solution was mixed with the fuel ultrasonically using the U400 ultrasonicator.
- the generator was operated at a constant 1510 rpm.
- a 2° C. rise in block temperature was noted during the test which included the scavenger.
- a summary of the exhaust fumes can be seen in Table 4.
- the scavenger solution of Example 3 was tested in red diesel in an amount of 500 ppm. A comparison was made with red diesel without the scavenger solution.
- Composition 7 was mixed with water and heavy fuel oil in the amounts set out in Table 7.
- the mixture was emulsified using a UIP1000 bench top ultrasonicator from Hielscher.
- Table 7 sets out the power required to produce a stable emulsion.
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Abstract
Description
- This invention relates to compositions suitable for use as emulsifiers or scavengers and to diesel formulations or emulsions containing the compositions.
- Diesel engines are very efficient engines. However, the use of diesel fuel presents a number of difficulties. In particular, diesel engines produce a significant amount of regulated pollutants, including particulate matter, NOx, SOx and CO.
- It is known that water-emulsified diesel can improve the physical or chemical properties of the diesel and reduce some of the pollutant emissions. Lif and Holmberg “Water-in-diesel emulsions and related systems”, Advances in Colloid and Interface Science, 123-126 (2006), pp 231-239 provides background of the use of water-emulsified diesel and other related fuels.
- However, in order to obtain the benefits of the water-emulsified diesel, it is important that the resulting emulsion is stable. Diesel engines are used in a wide variety of different conditions. Therefore, the emulsion needs to be stable across an extremely broad temperature range (such as −20 to 70° C.). Al-Sabagh et al “Formation of water-in-diesel oil nano-emulsions using high energy method and studying some of their surface active properties” Egyptian Journal of Petroleum (2011) 20, pp 17-23 discusses the use of ultrasound to prepare stable emulsions using Span 80, Emarol 85 and their mixture as emulsifiers. WO2013/098630 discloses diesel oil and water emulsions and discusses the importance of stability of at least 3 months under normal storage conditions and at temperatures between −20 and +50° C. However, there is no evidence of an improved stability. WO03/075954 discloses and emulsifying composition comprising an ethoxylated alkylphenol, a fatty acid amine, oleic acid and naphtha.
- It is usual to include an emulsifier in the water-diesel emulsion. However, typical emulsions still do not have sufficient stability.
- It would be desirable to introduce a composition which could provide stable micro- or nano-emulsions.
- Diesel fuels typically contains large amounts of sulphur, which results in the production of SOx. There is a move to reduce the amount of sulphur present in diesel. However, reducing the amount of sulphur also reduces the lubricity of the diesel, which causes problems in the engine, as discussed in Uchoa et al, “Evaluation of Lubricating Properties of Diesel Based Fuels Micro Emulsified With Glycerin”, Materials Research, 2017, 20(Suppl. 2), pp 701-708. This is commonly remedied by including bio-ingredients into the diesel fuel. However, the inclusion of these bio-ingredients can cause problems with the formation of stable nano-emulsions.
- Therefore, it would be desirable to provide a diesel fuel composition which had good lubricity whilst at the same time providing stable nano-emulsions.
- Compositions which are capable of forming stable nano-emulsions in standard diesel are not typically capable of forming stable nano-emulsions in ultra low sulphur diesel with bio-ingredients and vice versa.
- It would be desirable to provide a composition which can be added to either type of diesel or to heavy fuel oil and provide various benefits including reduced emissions without the need to add additional water.
- It would further advantageous to provide a composition which can be tailored easily to produce stable nano-emulsions in diesel fuels containing different amounts of sulphur and different amounts of bio-components.
- It would be advantageous to provide compositions which can be tailored to improve different properties of the emulsions, including lubricity, droplet size, corrosion resistance and specific gaseous and particulate emissions.
- It would be additionally advantageous to provide a composition which is capable of producing a stable nano-emulsion at low levels of power input and/or very quickly.
- For the purposes of the present invention, reference to diesel or diesel fuel is intended to cover petroleum diesel, low-sulphur diesel, biodiesel and combinations thereof.
- For the purposes of the present invention, reference to petroleum diesel relates to diesel produced during the distillation of crude oil.
- For the purposes of the present invention, reference to heavy fuel oil relates to oil produced during the distillation of crude oil and having a density greater than 900 kg/m3 at 15° C.
- For the purposes of the present invention, reference to low-sulphur diesel relates to diesel having less than 500 ppm, preferably less than 50 ppm, and most preferably less than 10 ppm sulphur. Low-sulphur diesel can be produced by removing the sulphur from petroleum diesel, by the formation of synthetic diesel or by the formation of biodiesel.
- For the purposes of the present invention, reference to biodiesel relates to fatty acid methyl ester obtained by transesterification of vegetable oils or animal fats with an alcohol, typically methanol or ethanol.
- For the purposes of the present invention, reference to bio-components relates to biodiesel and naturally occurring oils, such as palm oil, rapeseed oil and coconut oil.
- In a first aspect of the present invention, there is provided an emulsifier which is capable of forming a stable emulsion with diesel or heavy fuel oil. The emulsifier comprises:
-
- a. at least one C8 to C18 fatty acid diethanolamide;
- b. at least one C12 to C24 fatty acid; and
- c. at least one C6 to C18 alcohol ethoxylate.
- Preferably, the emulsifier does not comprise or contain naphtha. Preferably, the emulsifier consists essentially of components (a), (b) and (c).
- The emulsifier is suitable to be used to form an emulsion with diesel, low sulphur diesel, biodiesel or heavy fuel oil. The emulsion can comprise up to 30 wt % water. The emulsion comprises at least 0.5 wt % emulsifier. Higher levels of emulsifier can be used up to 15 wt %. However, increasing the amount of emulsifier increases the cost with no identifiable improvement in stability. Therefore, a preferred upper limit for the amount of emulsifier is 3 wt %. It is preferred that the emulsion contains only the fuel, water and the emulsifier.
- It is preferred that the fatty acid diethanolamide is a formed from a mixture of fatty acids having from 8 to 18 carbon atoms. It is particularly preferred that the fatty acid diethanolamide is derived from a natural source. Suitable natural sources include coconut oil and palm oil. By way of example, coconut oil is a mixture of acids including caprylic, capric, lauric, myristic, palmitic, stearic, oleic and linoleic acids.
- One feature of components used in emulsifiers is the HLB. HLB values can either be calculated or determined experimentally. The standard methods of calculation include those of Griffin (Journal of the Society of Cosmetic Chemists 5 (1654): 259) or Davies (Gas/Liquid and Liquid/Liquid interface: Proceedings of the International Congress of the Surface Activity (1657). However, it is preferred that the HLB values are obtained experimentally. It is usual for suppliers of materials to provide HLB values for their products which are obtained experimentally. The skilled person is aware of suitable methods to determine the HLB value, such as using comparative testing by forming a series of emulsions with an emulsifier and an oil of known HLB value. In general, a HLB in the range of 3.5 to 6 is commonly used for water in oil emulsions. A HLB in the range of 8 to 18 is used for oil in water emulsions.
- Coconut oil diethanolamide typically has a HLB in the range of 13-14. Whilst it is not essential that the diethanolamide has an HLB in this range, it is preferred that the diethanolamide has an HLB in the range of 11-16 and preferably 13-14.
- Fatty acid diethanolamides based on fatty acids with fewer than 8 carbon atoms or more than 18 carbon atoms can optionally be present in the mixture, although it is preferred that they are not.
- It is preferred that the fatty acid diethanolamide is present in an amount of from 40 to 90 wt % of the emulsifier. It is more preferred that it is present in an amount of from 50 to 90 wt % and more preferably from 60 to 85 wt %.
- The at least one C12 to C24 fatty acid is preferably saturated or monounsaturated, with monounsaturated fatty acids being further preferred. The fatty acid is preferably a C14-20 monounsaturated fatty acid. A particularly suitable fatty acid is oleic acid.
- Oleic acid has a HLB of approximately 1. A low HLB means that it is highly lipophilic and therefore a material of this lipophilicity is not typically used as an emulsifier. It is preferred that the fatty acid has a low HLB, preferably below 3.5 and more preferably below 2.
- The fatty acids are preferably present in an amount of from 1 to 15 wt %, more preferably from 2 to 10 wt % and most preferably from 4 to 7 wt % of the emulsifier.
- The C6 to C18 alcohol ethoxylate is preferably produced from at least one alcohol and more preferably at least one mono-ol. The ethoxylates preferably have from 2 to 8 ethoxy-groups. Preferred ethoxylates include nonylphenol ethoxylate and C9-C12 ethoxylates. Suitable ethoxylates are commercially available. Suitable ethoxylates include Berol 260 and Ethylan 1005, which are narrow range ethoxylated alcohols commercially available from AkzoNobel.
- Nonylphenol ethoxylates have a range of HLB values depending on the number of ethylene oxide groups present. Preferred nonylphenol ethoxylate have from 4 to 8 ethylene oxide groups, which have an HLB of approximately from 9 to 12. A particularly preferred nonylphenol ethoxylate has 6 ethylene oxide groups and a HLB of approximately 11.
- Berol 260 has a HLB value of 10.5 and is a narrow range C9-11 alcohol with 4 ethylene oxide groups. Ethylan 1005 has a HLB value of 11.6 and is a narrow range C10 alcohol with 3.5 ethylene oxide groups.
- It is preferred that the alcohol ethoxylate has a HLB value in the range of 9 to 12 and preferably from 10 to 12.
- The alcohol ethoxylate is preferably present in an amount of from 5 to 30 wt % of the emulsifier. It is further preferred that the alcohol ethoxylate is present in an amount of from 5 to 20 wt % and more preferably from 8 to 12 wt %.
- The emulsifier can optionally comprise a sorbitan ester as defined below. The sorbitan ester, where present, is used in an amount of from 10 to 40 wt % of the emulsifier, preferably from 20 to 30 wt %.
- In a second aspect of the present invention, there is provided an emulsifier which is suitable for forming a stable nano-emulsion of diesel and water, wherein the diesel does not contain any bio-components.
- The emulsifier comprises:
-
- a. 60-90 wt % of at least one C8 to C18 fatty acid diethanolamide;
- b. 2-10 wt % of at least one C12 to C24 fatty acid; and
- c. 5-20 wt % of at least one C6 to C18 alcohol ethoxylate.
- Preferred components a to c are as defined above.
- Preferably, the emulsifier does not comprise naphtha. Preferably, the emulsifier consists essentially of components (a), (b) and (c).
- The nano-emulsion comprises a fuel comprising at least one of petroleum diesel, low sulphur diesel and heavy fuel oil, wherein the fuel does not contain any bio-components, wherein the fuel does not contain any bio-components, up to 20 wt % water and the emulsifier, wherein the emulsifier:water volume ratio is from 1.5:1 to 1:2.9, and preferably 1.2:1 to 1:2. It is preferred that the water is present in an amount of at least 0.25 wt % and more preferably at least 0.5 wt %. It is preferred that the nano-emulsion contains only the fuel, water and emulsifier. Although other components can be present, it is preferred that these are only present in trace amounts of less than 0.1 wt %.
- In a preferred embodiment, the emulsifier of the second aspect comprises 80-90 wt % of component a, 4-8 wt % of component b and 5-15 wt % of component c.
- In a third aspect of the present invention, there is provided an emulsifier which is suitable for forming a stable nano-emulsion of diesel and water, wherein the diesel contains bio-components.
- The emulsifier comprises:
-
- a. 50-75 wt % of at least one C8 to C18 fatty acid diethanolamide;
- b. 2-10 wt % of at least one C12 to C24 fatty acid;
- c. 5-20 wt % of at least one C6 to C18 alcohol ethoxylate; and
- d. 10-40 wt % of at least one sorbitan ester.
- Preferably, the emulsifier does not comprise or contain naphtha. Preferably, the emulsifier consists essentially of components (a), (b), (c) and (d).
- The nano-emulsion comprises a fuel comprising at least one of diesel, low sulphur diesel, biodiesel and heavy fuel oil, wherein the fuel comprises bio-components, up to 20 wt % water and the emulsifier of the third aspect. The emulsifier:water volume ratio is from 1.5:1 to 1:2.9, and preferably 1.2:1 to 1:2. It is preferred that the nano-emulsion contains only the fuel, water and emulsifier. Although other components can be present, it is preferred that these are only present in trace amounts of less than 0.1 wt %.
- Preferred components a to c are as defined above.
- The sorbitan ester is the reaction product of sorbitan and one or more carboxylic acids. Preferably, the carboxylic acids have from 8 to 22 carbon atoms. Preferably the carboxylic acids have from 8 to 22 carbon atoms, which is the length of carbon chains found in naturally occurring fatty acids in triglycerides. Particularly preferred are carboxylic acids having from 16 to 22 carbon atoms and even more preferably having 18 carbon atoms. The fatty acids can be both linear and branched.
- Both saturated and unsaturated fatty acids are suitable. However, unsaturated fatty acids are preferred.
- Some sorbitan esters which are suitable for use in the present invention include:
-
Ester HLB Sorbitan tristearate 2.1 Sorbitan monooleate 4.3 Sorbitan isostearate 4.7 Sorbitan trioleate 1.8 Sorbitan sesquioleate 3.7 - Suitable sorbitan esters have an HLB of less than 6.0. Preferred sorbitan esters are those having an HLB of from 3 to 5. Particularly preferred is sorbitan monooleate.
- In a preferred embodiment, the emulsifier of the second aspect comprises 55-65 wt % of component a, 4-8 wt % of component b, 5-15 wt % of component c and 20 to 30 wt % of component d.
- In a fourth aspect, there is provided a scavenger solution. The scavenger solution is capable of being added to diesel or heavy fuel oil. The scavenger solution is capable of emulsifying any residual water in the diesel as well as improving the lubricity of the diesel. By removal of residual water, the scavenger is capable of providing other benefits including preventing diesel bug. In one embodiment, the scavenger solution comprises:
-
- a. 10-25 wt % of at least one C8 to C18 fatty acid diethanolamide;
- b. 0.2-3 wt % of at least one C12 to C24 fatty acid;
- c. 1-4 wt % of at least one C6 to C18 alcohol ethoxylate; and
- d. 60-90 wt % alkylene glycol monoalkyl ether.
- Preferably, the scavenger solution does not comprise or contain naphtha Preferably, the scavenger solution consists essentially of components (a), (b), (c) and (d).
- In a second embodiment, the scavenger solution comprises from 10 to 40 wt % of the emulsifier of any one of the first to third aspects of the present invention and from 60 to 90 wt % alkylene glycol monoalkyl ether.
- A fuel formulation is formed of a fuel comprising at least one of diesel, low sulphur diesel, biodiesel and heavy fuel oil and the scavenger solution in an amount of 0.03 to 0.2% by volume and preferably 0.03 to 0.075% by volume. The inclusion of the scavenger in the above amounts is capable of treating a fuel with up to 5 wt % of residual water. However, it is preferred that the water contains less than 2.5 wt % and more preferably less than 1 wt % water.
- It is preferred that the fuel formulation contains only the fuel, water and emulsifier. Although other components can be present, it is preferred that these are only present in trace amounts of less than 0.1 wt %.
- Preferred components a to c are as defined above.
- The alkylene glycol monoalkyl ether is preferably an ethylene glycol monoalkyl ether and more preferably an ethylene glycol monoalkyl ether in which the alkyl group has from 1 to 6 carbon atoms. More preferably, the ether is preferably 2-butoxyethanol (butyl oxitol).
- The alkylene glycol monoalkyl ether is preferably used in an amount of 70 to 90% by weight and more preferably from 75 to 85% by weight.
- The emulsifiers of the present invention advantageously permit emulsions of diesel and heavy fuel oils to be formed easily with low levels of emulsification energy. The resulting emulsions produced are stable for long periods of time. The emulsions also provide the advantageous properties of water in diesel emulsions by reducing the amount of emissions and particulates produced. These emulsifiers, which can be produced using naturally occurring materials, are therefore beneficial as they are environmentally beneficial as they do not typically contain components which are harmful to produce whilst at the same time reducing emissions in the engines in which they are used.
- Emulsions can be formed irrespective of the order of the addition. It is possible to add the emulsifier to the diesel or heavy fuel oil and then add water, to add the emulsifier to a mixture of diesel or heavy fuel oil and water or to add a mixture of emulsifier and water to the diesel or heavy fuel oil.
- In a further aspect of the present invention, there is provided a mixture of an emulsifier according to any one of the above aspects of the present invention and water. The mixture comprises water and emulsifier in the relative amounts described above in the absence of the diesel or heavy fuel oil.
- In a fifth aspect, there is provided a method of making a nano-emulsion comprising emulsifying a mixture of fuel, water and an emulsifier of the second, third or fourth embodiments using ultrasonic emulsification.
- The use of ultrasonic emulsification to produce nano-size emulsions is known to the skilled person and is described for example in Hielscher, “Ultrasonic Production of Nano-Size Dispersions and Emulsions, ENS'05, 14-16 Dec. 2005.
- One benefit of forming a nano-emulsion using ultrasonic emulsification is the speed at which the emulsions can be produced. The emulsions can be formed in seconds rather than minutes.
- In addition, nano-emulsions of water in diesel have been shown to be effective for use in diesel engines at reducing the level of toxic emissions.
- However, improved properties are only beneficial if the resulting nano-emulsions are stable for long periods of time and at varying temperatures. Stability of the emulsions is important as a change in properties of a fuel is problematic as it will have a great impact on the levels of emissions produced.
- The emulsions of the present invention are not only highly stable, but the nano-emulsions can be produced using surprisingly low levels of energy, which is commercially and environmentally advantageous.
- Whilst the scavenger solution of the fourth aspect can be used to produce nano-emulsions, it is preferred that the emulsion is produced by simple addition of the scavenger solution to the fuel. The emulsions can be formed by simple mixing of the scavenger solution and fuel. In one preferred embodiment, the emulsion can form in situ as the fuel passes through the fuel pump.
- The emulsifier or scavenger compositions of any of the first to fourth aspects can optionally contain other components. The inclusion of the components is generally known to the skilled person and they are used in their usual amounts.
- Metal oxides are known to be useful for reducing SOx and NOx. Where used, these are typically present in the compositions in amounts of from 5 to 100 ppm. Suitable metal oxides include cerium oxide, magnesium oxide, titanium oxide, iron oxide and aluminium oxide. Magnesium oxide is typically used in heavy fuel oils and cerium oxide is typically used in diesel.
- Ferrocene is also known to the skilled person to be useful for promoting smokeless combustion of fuels.
- Lower (C1-5) alcohols are commonly used to reduce soot and also to reduce the freezing point of the diesel or heavy fuel oil composition. Preferred alcohols include methanol, ethanol, i-propanol and n-propanol. These are used in an amount of less than 5% by weight and more preferably less than 2% by weight.
- Stability of the emulsions is important. A simple emulsion of water and diesel will slowly separate. The inclusion of emulsifiers is therefore intended to improve the stability. One measure of the stability of the emulsion is the droplet size. This can be measured by looking at the turbidity, which can be measured using a Turbimeter, such as a Van Walt Compact Turbimeter. Therefore, turbidity can be used as a means of studying the stability of an emulsion.
- In addition, the turbidity can be used to assess how effective an emulsifier is at forming an emulsion i.e. the relative ability of an amount of emulsifier to form an emulsion. The smaller the particle size for a specific amount of emulsifier, the more effective that emulsifier is.
- Measurement of turbidity is a quick method to establish the effectiveness of an emulsifier.
- The invention will be further described with reference to the following Figures:
-
FIG. 1 shows the stability of diesel emulsions over a year; -
FIG. 2 shows the stability of a diesel emulsion when cooled to −20° C.; -
FIG. 3 shows the stability of a diesel emulsion when heated to 70° C.; -
FIG. 4 shows the stability of a heavy fuel oil emulsion after 9 months. - The invention will be further described with reference to the following Examples.
- A number of compositions were produced and tested for producing emulsions with varying amounts of water. Each composition was produced by mixing the emulsifier, blending the emulsifier with diesel and then adding water and emulsifying.
- The emulsifiers were made using the following ingredients:
- Coconut fatty acid diethanolamide (CDE) from by SABO®
- Oleic acid (OE) from Eastman Chemical Company
- Tergitol® NP-6 (nonylphenol polyethoxylate) (NP-6D) by The Dow Chemical Company
- Nonylphenol polyethoxylate (NP-6G) by Gamma Chemical
- Sorbitan monooleate (SPAN 80) by CRODA®
- Berol 260 (C9-11 alcohol ethoxylate) (B260) by AkzoNobel®
- Ethylan 1005 SA (C10 alcohol ethoxylate) (E1005) by AkzoNobel®
- The emulsifiers used the following parts by weight.
-
TABLE 1 Composition CDE OA NP-6D NP-6G SPAN 80 1* 30 20 50 2* 45 27 28 3* 65 10 25 4* 75 12 13 5 65 25 10 6 80 10 10 7 85 5 10 8 62.5 10.5 8 19 9 62 5 10 23 10 65 5 10 20 *indicates an example not within the scope of the claims - 3 parts by weight of emulsifier were mixed with 89 parts by weight of diesel and water in the amounts set out in Table 2. The emulsions were formed using the specified mixer and the turbidity measured.
-
TABLE 2 Composition 1* 2* 3* 3* 4* 5 6 7 8 9 10 Diesel Local Local Local Shell Local Shell Shell Shell Shell Shell Shell V-Power V-Power V-Power V-Power 50 50 50 Mixer SC SC SC U1000 SC U1000 U1000 U1000 U400 U400 U400 Turbidity @0 0.74 0.01 0.01 0.01 0.01 parts H2O @1 part H2O 0.42 0.82 >1050 4.15 4.54 4.28 0.01 1.82 2.09 @2 parts H2O 11.1 7.95 4.11 27.50 23.10 30.20 13.6 8.3 35.1 @3 parts H2O 30.5 28.1 20.6 29.6 50.80 46.60 19.1 17.5 27.9 @4 parts H2O 50.0 51.2 41 42.8 50.5 50.6 24.7 51.2 43.7 @5 parts H2O 50.9 51.3 700.0 50.5 50.6 50.7 38.8 855 50.7 @6 part H2O 58.5 51.5 0.74 50.6 50.6 45.6 72.4 >1050 405 @7 parts H2O 90.5 58.6 67 68.4 55.3 412 >1050 429 @8 parts H2O >1050 145 100 134 76.8 76.8 351 329 682 @12 parts H2O 200 @15 parts H2O 320 *indicates an example not within the scope of the claims - SC is a Heidolph Silent Crusher variable speed high shear mixer.
- U1000 is a Hielscher UIP1000 bench top ultrasonicator.
- U400 is a Hielscher UP400st lab ultrasonicator.
- Both “local” diesel and Shell V-Power are both diesel fuels that do not contain bio components.
- Shell 50 is Shell V Power 50 ppm diesel which has less than 50 ppm sulphur and contains bio-components.
- Turbidity was measured immediately after the formation of the emulsion using the Van Walt Compact Turbimeter.
- The results demonstrate that the compositions of the present invention are capable of forming stable emulsions with low turbidity across a broad range of water content using low levels of the compositions. The compositions are also capable of forming stable emulsions even when the fuel is a low sulphur fuel.
- Compositions were tested to measure the stability of emulsions of water and diesel containing biocomponents at higher levels of water.
- Composition 10 was mixed with water at a ratio of 33 parts composition to 67 parts by weight water. The mixture of water and composition were then added to Shell 50 in the amounts set out in Table 3. The mixing was undertaken at ambient temperature. The diesel/water mixture was emulsified using a U400 ultrasonicator for 1 minute. The samples were then allowed to cook to ambient temperature and transferred to a container for long term storage. The container was stored at ambient temperature at an altitude of 550 m. The ambient temperature varied from 0° C. to 37° C.
- The turbidity was measured immediately after emulsification and again after a few minutes once air bubbles had cleared.
-
TABLE 3 Shell 50 Water/Example 10 Turbidity @0 Turbidity @2-5 (pbw) (pbw) mins mins 90 10 60.5 50.3 85 15 71.3 50.4 80 20 155 50.5 - The emulsions were stored for a period of greater than a year. It should be noted that storage of modern fuels for more than 6 months is not recommended. All three emulsions were stable for a year. After 15 months, the emulsion containing 10 pbw water/emulsifier had separated slightly. This was the time when the first signs of separation had started to show. 15 months is an extremely long period of stability. This is shown in
FIG. 1 , in which a) shows the emulsions at formation (water/emulsifier content from left to right 20, 15, 10) and b) shows the emulsions after 15 months (same order) in which the emulsion for 10 pbw water is more turbid. - 5 parts by weight of Example 10 was mixed with 85 parts by weight of diesel and 10 parts by weight of water. The diesel/water/emulsifier mixture was emulsified using a U400 ultrasonicator for 1 minute. The samples were placed in a heated oven at 70° C. for 1 hour and returned to ambient temperature. The same samples were placed in a freezer at −20° C. for an hour and returned to ambient temperature.
- The samples are shown in
FIGS. 2 and 3 . - It can be seen that in
FIG. 2a , at −20° C., the emulsion is turbid. However, inFIG. 2b , the emulsion is clear after returning to ambient temperature without any stirring. - Similarly, in
FIG. 3a , at 70° C., the emulsion is turbid. However, inFIG. 3b , the emulsion is clear after returning to ambient temperature without stirring. - 1 part by weight of the composition of Example 7 was mixed with 30 parts by weight of water and 69 parts by weight of heavy fuel oil at 70° C. and emulsified using a U400 ultrasonicator for 3.5 minutes. The samples were then allowed to cool to ambient temperature and transferred to a container for long term storage. The container was stored at ambient temperature at an altitude of 550 m. The ambient temperature varied from 0° C. to 37° C.
- The resulting emulsion remained stable for over 9 months.
FIG. 4 shows the emulsion of the heavy fuel oil and water after 9 months. - A scavenger solution was prepared using Composition 7. 1 part by weight of this composition was mixed with 4 parts by weight of butyl oxitol.
- Testing was undertaken on Shell 500 ppm sulphur diesel in a diesel generator. The diesel generator was a 229-3 3 cylinder generator from MWM Motores Diesel Ltda.
- Emissions were tested for the fuel as a baseline measurement and for the fuel containing 500 ppm of the scavenger solution.
- The scavenger solution was mixed with the fuel ultrasonically using the U400 ultrasonicator. The generator was operated at a constant 1510 rpm. A 2° C. rise in block temperature was noted during the test which included the scavenger. A summary of the exhaust fumes can be seen in Table 4.
-
TABLE 4 O2 CO CO2 NO NOx NO2 SO2 Temp ° C. % ppm % ppm ppm ppm ppm m3/s m/s Shell 50 112.14 18.46 633.4 1.61 133.6 191.7 55.9 21.7 17.3 7.7 Shell 50 + 500 107.50 19.23 445.5 1.11 89 146.8 45.2 17.0 24.4 10.8 ppm scavenger - The results show a marked reduction in the amount of CO, NOx and SOx when operating with the fuel which contained the scavenger.
- A test was also run on the above two fuels to measure the opacity of the exhaust gas. This measurement is related to the amount of particulate in the exhaust gas. Testing was undertaken using a Texa Diesel Smoke Opacimeter. The Opacimeter provides a qualitative and partially quantitative assessment of the amount of particulate in the exhaust gas. The baseline test gave an opacity result in the range of 1.6 to 2.3%. Testing using the fuel containing the scavenger showed a 100% reduction in the opacity i.e. showed 0% opacity.
- It can be seen that addition of the scavenger reduces the all of the emissions including particulate emissions.
- The scavenger solution of Example 3 was tested in red diesel in an amount of 500 ppm. A comparison was made with red diesel without the scavenger solution.
- The emissions were tested from a diesel tractor and the diesel generator used in Example 3.
- The results are shown in Tables 5 and 6.
-
TABLE 5 Diesel + 500 ppm Parameter Units Diesel Scavenger Total Particulate Matter mg/m3 45.3 41.5 Total Particulate emission rate g/hr 5.3 4.8 PM 10 mg/m3 12.2 5.7 PM 10 emission rate g/hr 1.0 0.5 PM 2.5 mg/m3 10.63 4.1 PM 2.5 emission rate g/hr 0.91 0.4 NO2 mg/m3 655.1 697.1 NO2 emission rate g/hr 75.3 80.1 SO2 mg/m3 26.1 26.1 SO2 emission rate g/hr 3.0 3.1 CO mg/m3 903.1 763.2 CO emission rate g/hr 103.8 87.7 CO2 % v/v 2.13 2.10 O2 % v/v 17.95 17.98 Moisture % 3.8 3.0 Stack gas temperature ° C. 113 113 Stack gas velocity m/s 19.1 19.1 -
TABLE 6 Diesel + 500 ppm Parameter Units Diesel Scavenger Total Particulate Matter mg/m3 16.9 14.4 Total Particulate emission rate g/hr 4 3.5 PM 10 mg/m3 PM 10 emission rate g/hr PM 2.5 mg/m3 PM 2.5 emission rate g/hr NO2 mg/m3 397.8 399.2 NO2 emission rate g/hr 100.8 101.2 SO2 mg/m3 19.5 21.6 SO2 emission rate g/hr 4.9 5.5 CO mg/m3 80.9 86 CO emission rate g/hr 20.5 21.8 CO2 % v/v 2.37 2.3 O2 % v/v 17.79 17.89 Moisture % 6.9 3.9 Stack gas temperature ° C. 117 117 Stack gas velocity m/s 25.6 25.6 - It can be seen that in both cases, there is a reduction in the total level of particulate matter produced with the addition of the additive.
- Composition 7 was mixed with water and heavy fuel oil in the amounts set out in Table 7. The mixture was emulsified using a UIP1000 bench top ultrasonicator from Hielscher.
- Table 7 sets out the power required to produce a stable emulsion.
-
TABLE 7 HFO (g) Composition 7 (g) Water (g) Power (Ws/g) 80 1 5 31.4 80 1 9 42.8 80 1 18 61.3 80 2 18 8.0 - It can be seen from Table 7 that it is possible to produce a stable emulsion in all cases. However, when an emulsion is produced using 2% of Composition 7 in combination with 18% of water, it is possible to produce an emulsion at significantly lower levels of power. This low level of power is particularly useful as the cost for producing the emulsion is relatively low. Given the energy saving and reduction in emissions identified above when using water/heavy fuel oil emulsions, it can be seen that the present invention provides a commercially beneficial method and emulsion.
- It is expected that this process will enable higher levels of water to be emulsified whilst requiring a low amount of power. The skilled person is capable of refining the specific amounts of the composition and the water.
- In this specification, unless expressly otherwise indicated, the word ‘or’ is used in the sense of an operator that returns a true value when either or both of the stated conditions is met, as opposed to the operator ‘exclusive or’ which requires that only one of the conditions is met. The word ‘comprising’ is used in the sense of ‘including’ rather than in to mean ‘consisting of’. All prior teachings acknowledged above are hereby incorporated by reference. No acknowledgement of any prior published document herein should be taken to be an admission or representation that the teaching thereof was common general knowledge in Australia or elsewhere at the date hereof.
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2217229A (en) * | 1988-04-25 | 1989-10-25 | Enersolve Chemical Company Lim | Solubilising composition |
WO2001010982A1 (en) * | 1999-05-27 | 2001-02-15 | Aae Holdings Plc | Compositions |
US20030159339A1 (en) * | 2003-03-03 | 2003-08-28 | Alan Rae | Fuel additive |
US20050223628A1 (en) * | 2002-03-08 | 2005-10-13 | Mawdsley Michael J | Fuel additive |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9621753D0 (en) | 1996-10-18 | 1996-12-11 | Williamson Ian V | Fuel composition |
US6716801B2 (en) * | 1997-05-02 | 2004-04-06 | Pauline Abu-Jawdeh | Compositions and method for their preparation |
JP2001011477A (en) | 1999-06-30 | 2001-01-16 | Goro Ishida | Surface active agent composition and emulsified fuel containing the same |
EP1257618A1 (en) * | 2000-02-26 | 2002-11-20 | AAE Technologies International Limited | Fuel additive |
US7357819B2 (en) * | 2001-05-07 | 2008-04-15 | Victorian Chemicals International Pty Ltd | Fuel blends |
JP2008255208A (en) | 2007-04-04 | 2008-10-23 | Masayuki Furuno | Additive for water-solubilized oil, method for producing the same additive, and method for producing water-solubilized oil by using the same additive |
JP5781745B2 (en) | 2010-04-28 | 2015-09-24 | 田川 和男 | Oil / water solubilizer, method for producing the same, and mixed fuel |
ITRM20110694A1 (en) | 2011-12-29 | 2013-06-30 | Fuel S A E | STABILIZED EMULSIONS WITH WATER-EFFECTIVE DIESEL OIL. |
JP6463125B2 (en) | 2014-12-24 | 2019-01-30 | ミヨシ油脂株式会社 | Emulsion fuel |
JP6393223B2 (en) | 2015-03-25 | 2018-09-19 | 株式会社ネオス | Emulsifier for water emulsion fuel and water emulsion fuel containing the same |
CN108165301B (en) * | 2017-11-17 | 2020-12-25 | 南京尚易环保科技有限公司 | Water removing agent for diesel oil |
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2217229A (en) * | 1988-04-25 | 1989-10-25 | Enersolve Chemical Company Lim | Solubilising composition |
WO2001010982A1 (en) * | 1999-05-27 | 2001-02-15 | Aae Holdings Plc | Compositions |
US20050223628A1 (en) * | 2002-03-08 | 2005-10-13 | Mawdsley Michael J | Fuel additive |
US20030159339A1 (en) * | 2003-03-03 | 2003-08-28 | Alan Rae | Fuel additive |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116556084A (en) * | 2023-05-30 | 2023-08-08 | 常州保洁洗涤剂制造有限公司 | One-step energy-saving auxiliary agent for cone dyeing and preparation method thereof |
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